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Healix Advance

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 222316Model General Orthopedic Use Awls, Taps, and Reamers

by Medos International Sàrl

Identity

Trade Name
HEALIX ADVANCE Cortical Awl-Tap EUDAMED
HEALIX ADVANCE FDA UDI
Generic Name
Bone awl, reusable FDA UDI
Device Name
Awl, Tap, Reamer, Femoral, Tibial, Cortical, Arthroscopic, Healix, Healix Advance, GII, Gryphon, Milagro EUDAMED
HEALIX ADVANCE Cortical Awl-Tap Package Contains: 1 Cortical Awl-Tap 4.5mm FDA UDI
Model / Reference
222316 EUDAMEDFDA UDI
General Orthopedic Use Awls, Taps, and Reamers EUDAMED
Description
HEALIX ADVANCE Cortical Awl-Tap Package Contains: 1 Cortical Awl-Tap 4.5mm FDA UDI

Identifiers

Catalog Number
222316 FDA UDI
Primary DI / UDI-DI
10886705022410 EUDAMEDFDA UDI
Basic UDI-DI
0886705a00121K4 EUDAMED
Direct Marketing DI
10886705022410 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
Z12139099 VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - OTHER EUDAMED
GMDN Term
Bone awl, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone awl, reusable

Healix Advance by Medos International Sàrl — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bone awl, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI e57b3e44-5af2-4799-89c2-9f35b8bd4cfa 35 fields · synced Jul 10, 2026
  • EUDAMED 8eda7901-ff75-4cef-8b69-eba11b434b01 61 fields · synced Jul 10, 2026